Highly selective and sensitive streptomycin chemiluminescence sensor based on aptamer and G-quadruplex DNAzyme modified three-dimensional graphene composite

[Display omitted] •Aptamer and G-quadruplex DNAzyme modified three-dimensional graphene was successfully prepared.•The introduction of aptamer improved the selectivity of the sensor.•G-quadruplex DNAzyme improved the sensitivity of the sensor.•The chemiluminescence sensor was successfully used to de...

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Veröffentlicht in:Sensors and actuators. B, Chemical Chemical, 2019-12, Vol.301, p.127122, Article 127122
Hauptverfasser: Sun, Yuanling, Han, Rui, Dai, Yuxue, Zhu, Xiaodong, Liu, Hao, Gao, Dandan, Luo, Chuannan, Wang, Xueying, Wei, Qin
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Sprache:eng
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Zusammenfassung:[Display omitted] •Aptamer and G-quadruplex DNAzyme modified three-dimensional graphene was successfully prepared.•The introduction of aptamer improved the selectivity of the sensor.•G-quadruplex DNAzyme improved the sensitivity of the sensor.•The chemiluminescence sensor was successfully used to detect streptomycin in cucumber and milk samples. In our work, a highly selective and sensitive streptomycin (STR) chemiluminescence (CL) sensor was successfully prepared based on aptamer and G-quadruplex DNAzyme (G-DNAzyme) modified three-dimensional graphene composite. Initially, β-cyclodextrins and ionic liquids functionalized graphene oxide aerogel (β-CD/IL@GOGA) was successfully prepared and characterized, in which graphene oxide aerogel (GOGA) was used as a skeleton material and provided large specific surface area, β-CD rich in hydroxyl groups and IL containing lots of stable ions increased the biocompatibility and stability of the composite, respectively. Then, tetracycline aptamer (S-Apt) and G-DNAzyme was immobilized on the surface of β-CD/IL@GOGA, consecutively. Finally, G-DNAzyme/S-Apt/β-CD/IL@GOGA was used to construct the CL sensor for STR detection. S-Apt with specific recognition ability to its target and G-DNAzyme as a catalyst of luminol-H2O2 CL system improved the selectivity and sensitivity of the sensor, respectively. When STR existed, G-DNAzyme was released from the surface of S-Apt/β-CD/IL@GOGA due to the specific recognition and binding ability between STR and S-Apt, catalyzing the CL reaction. The CL sensor showed the linear range of 1.4 × 10−12 to 2.8 × 10−9 mol/L and detection limit of 9.2 × 10-14 mol/L (3δ). It was successfully used for STR detection in cucumber and milk samples.
ISSN:0925-4005
1873-3077
DOI:10.1016/j.snb.2019.127122